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MEF2A antibody (AA 453-479)

This Rabbit Polyclonal antibody specifically detects MEF2A in WB, IF and IHC (p). It exhibits reactivity toward Human and Mouse.
Catalog No. ABIN2842748

Quick Overview for MEF2A antibody (AA 453-479) (ABIN2842748)

Target

See all MEF2A Antibodies
MEF2A (Myocyte Enhancer Factor 2A (MEF2A))

Reactivity

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Human, Mouse

Host

  • 136
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Rabbit

Clonality

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Polyclonal

Conjugate

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This MEF2A antibody is un-conjugated

Application

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Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone

RB21291
  • Binding Specificity

    • 25
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    AA 453-479

    Predicted Reactivity

    B, Pig, Rat

    Purification

    This antibody is purified through a protein A column, followed by peptide affinity purification.

    Immunogen

    This MEF2A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 453-479 amino acids from the Central region of human MEF2A.

    Isotype

    Ig Fraction
  • Application Notes

    IF: 1:10~50. WB: 1:1000. IHC-P: 1:50~100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.

    Expiry Date

    6 months
  • Target

    MEF2A (Myocyte Enhancer Factor 2A (MEF2A))

    Alternative Name

    MEF2A

    Background

    MEF2A is a DNA-binding transcription factor that activates many muscle-specific, growth factor-induced, and stress-induced genes. The encoded protein can act as a homodimer or as a heterodimer and is involved in several cellular processes, including muscle development, neuronal differentiation, cell growth control, and apoptosis. Defects in this protein could be a cause of autosomal dominant coronary artery disease 1 with myocardial infarction (ADCAD1).

    Molecular Weight

    54811

    Gene ID

    4205

    NCBI Accession

    NP_001124398, NP_001124399, NP_001124400, NP_001165365, NP_005578

    UniProt

    Q02078

    Pathways

    Neurotrophin Signaling Pathway, Activation of Innate immune Response, Carbohydrate Homeostasis, Chromatin Binding, Regulation of Muscle Cell Differentiation, Toll-Like Receptors Cascades
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